Forkhead box protein P2 (FOXP2) is a protein that, in humans, is encoded by the FOXP2 gene. FOXP2 is a member of the forkhead box family of transcription factors, proteins that regulate gene …

The FOXP2 protein is active in several tissues, including the brain, both before and after birth. Studies suggest that the FOXP2 protein plays a key role in the functioning of synapses, which are the …

Nov 13, 2025 · FOXP2 (Forkhead Box P2) is a Protein Coding gene. Diseases associated with FOXP2 include Childhood Apraxia Of Speech and Language Disorder. Among its related pathways are Cell …

Aug 2, 2025 · While FOXP2 is recognized for its connection to human language, its functions extend to other species and developmental processes. This gene is found in many vertebrates, indicating a …

Children with the FOXP2-plus genetic condition, involving a deletion or duplication disrupting genes that neighbour FOXP2, may have associated learning, behavioural or social skill challenges.

Dec 1, 2024 · Genes regulated by FOXP2 are related to neural differentiation, connectivity, and synaptic plasticity, indicating its role in brain development and function. This review explores the intricate …

FOXP2 is a transcriptor protein which controls the activity of other genes. 1 FOXP2 is important for brain development (pre and post birth) and growth of nerve cells.

Transcription factor forkhead box protein P2 (FOXP2) plays an essential role in the development of language and speech. However, the transcriptional activity of FOXP2 regulated by the post …

The FOXP2 gene is one of the genes found on chromosome 7. When large deletions or rearrangements of genetic material on this chromosome affect the FOXP2 gene and neighboring genes, it can cause …

FOXP2 is defined as a transcription factor that modulates gene expression by binding to regulatory regions of target genes, influencing their transcription into messenger RNA, which is ultimately …